Introduction
Neurocysticercosis (NC) is caused by the larvae or cysticerci of Taenia solium. One of the most striking features of NC is its heterogeneous clinical picture, which can range from asymptomatic to severe life-threatening neurologic syndromes1. The disease severity and clinical manifestations are indicative of infective burden, location, and the host’s immune response2. In many developing countries, such as in our country, NC is a frequent medical condition, with reported frequencies as high as 9.1%3. The diagnosis of NC is made by neuroimaging techniques with either computer tomography (CT) or magnetic resonance imaging (MRI). Meanwhile, the lifetime probability of having invasive cancer is 39.7% for men and 37.6% for women. With an annual death rate of 168.3 per 100,000 population and an approximate cancer incidence of 418-502/100,000 population, cancer is one of the most common causes of mortality and morbidity4.
Information concerning NC and cancer is hardly found in medical literature. Some have suggested that the elicited chronic inflammatory reaction, evasive mechanisms, and molecular mimicry capacity of T. solium induce immunosuppression, which can be associated with cerebral gliomas1 and hematologic malignancies5. A postmortem study reported that 21% of patients with NC had a malignancy6, and some have proposed the pathogenic mechanisms7. The purpose of this study was to report the presentation of NC in patients with systemic cancer.
Methods
A database that was prospectively acquired from January 2012 to June 2017 was analyzed. All patients seen by the neuro-oncologic clinic of a referral cancer center (Instituto Nacional de Cancerología, Mexico City) were included. The demographic information, oncologic history, signs and symptoms, treatment, and median overall survival rates were collected. All patients had histopathologic confirmation of their primary cancer. The diagnosis of NC was made by a combination of clinical features and MRI. Active infection was diagnosed with the presence of active cysts in the vesicular, colloidal vesicular, and/or granular nodular stages on MRI. Overall survival was measured from the time of the first neuro-oncologic consultation until death or the last reported visit. The Institutional Ethics and Scientific Investigation Committees approved data acquisition and analysis.
Results
The general characteristics are presented in table 1. Of the 18 patients included in this study, 13 (72%) were women. The mean age was 61 ± 15 years (range, 36-85 years) at the time of cancer diagnosis and 58 ± 15 years (range, 25-84 years) at the time of NC diagnosis. During the study period, no patient developed Central Nervous System (CNS) metastases, and four patients developed metastases to sites other than the CNS (i.e., mediastinum, bone, lung, and suprarenal gland). The number of lesions seen on MRI was one or two in most patients (n = 13) and ≥3 in 5 patients, of which one patient presented with >100 lesions.
Patients characteristics | n = 18 (100%) |
---|---|
Gender | |
Female | 13 (72.2) |
Male | 5 (27.7) |
Primary site of cancer and stage | |
Breast | 5 (27.7) |
I (1) | |
II (2) | |
III (2) | |
Ovarian | 3 (16.6) |
NE (2) | |
IV (1) | |
Gastrointestinal | 2 (11.1) |
III (1) | |
IV (1) | |
Urologic | 3 (16.6) |
NE (1) | |
IV (2) | |
Skin/Melanoma | 3 (16.6) |
NE (1) | |
II (1) | |
III (1) | |
Lung | 1 (5.5) |
IV (1) | |
Head and Neck | 1 (5.5) |
IV (1) | |
Systemic metastases other than the CNS | |
Present | 4 (22.2) |
CNS metastases | |
Absent | 18 (100) |
Any clinical manifestation | 10 (55.5) |
Headache | 6 (33.3) |
Seizures | 4 (22.2) |
Intracranial hypertension | 3 (16.6) |
Visual impairment | 2 (11.1) |
Ataxia | 1 (5.5) |
Decreased awareness | 1 (5.5) |
None | 8 (44.4) |
Diagnosis of NC | |
Before the diagnosis of cancer (100-140 months) | 2 (11.1) |
After the diagnosis of cancer (2-191 months) | 16 (88.8) |
NE: Non-specified
The characteristics of the NC lesions are presented in table 2. Three patients showed signs of intracranial hypertension; two of them were treated with decompression surgery and, if considered by the neurosurgical team, excision of the intraventricular cysts, and one of them required three surgical interventions. During a mean follow-up period of 45.2 months (range, 1-147 months), eight deaths were reported. One patient who had a previous history of multiple NC reactivations developed NC recurrence and refractory status epilepticus; he died a month after the diagnosis. The other seven deaths were directly related to cancer progression. The median overall survival was 45 months (95% CI 21.7-68.6). Figure 1 illustrates the NCC findings on MRI. All patients with active infection received steroids, followed by albendazole at 15 mg/kg per day.
NC stage | No. of patients (%) | NC location (No.) | No. of lesions > 3 (5) | <3 (13) |
---|---|---|---|---|
Vesicular | 9 (50%) | ES 3 | 0 | 9 |
EI 1 | ||||
I 5 | ||||
Calcified nodular | 6 (33.3%) | ES 2 | 2 | 4 |
EI 1 | ||||
I 3 | ||||
Multiple (>2 stages) | 3 (16.6%) | ES 1 | 3 | 0 |
Both (E-I) 2 |
ES: extraparenchymal subarachnoid; EI: extraparenchymal intraventricular; I: intraparenchymal; E: extraparenchymal. No patient had granular nodular, colloidal vesicular, or non-cystic phases; NC: neurocysticercosis.
Discussion
T. solium cysticercosis is a globally reemerging disease, with an increasing number of cases in previously considered non-endemic countries, such as the USA, Canada, Australia, Japan, and Europe8,9. We presented 18 patients with NC who concurrently had systemic cancer; majority comprised women and had a mean age that was similar to that previously reported by others2. The most common symptoms that led to the diagnosis were headache and seizures. During follow-up, one of the patients died from NC-related complications, and seven died because of cancer progression. All patients were initially considered as having CNS metastases; MRI, other advanced techniques, such as positron emission tomography–computed tomography (PET/CT), and response to steroids/antiparasitic treatment helped in distinguishing NC from CNS metastases. MRI showed multiple NC lesions, and the most common finding was the vesicular stage.
Tapeworm infections have accompanied humans for more than 100,000 years. Characterization of the genomes of these parasites, as well as a deeper understanding of their molecular markers and the host–parasite relationship10, has improved diagnosis, treatment, and prevention. The diagnosis of NC is made by neuroimaging techniques, such as CT or MRI. The characteristics of NC vary according to the phases of development, including non-cystic, vesicular, colloidal vesicular, granular nodular, calcified nodular vesicular, and colloid to calcified stages. One of the known features of NC is the presence of multiple phases in the same patient11. Some have proposed a serologic test to confirm the diagnosis. The most recommended study is the enzyme-linked immunotransfer blot because of its high specificity and sensitivity in the context of active lesions. It uses purified glycoprotein antigens from T. solium in either cerebrospinal fluid (CSF) or serum samples. Enzyme-linked immunosorbent assays are better for CSF than for serum samples, but these are not fully recommended because of the poor specificity and sensitivity12. These serologic diagnostic studies are not used frequently and are not currently required for the diagnosis of NC13,14.
Some limitations should be considered in the present study. There may have been selection bias because it was done at a single cancer referral center, the studied population was high-risk, and only patients who were referred for neuro-oncologic consultation were included. To avoid information bias, all data had strict definitions, and all information was evaluated by the main author (BC). This study was not a population-based report and did not aim to review all of the MRI studies done at the institution to establish frequency.
Conclusion
In conclusion, although some have postulated that NC increases the risk of glioma and stroke, we consider that the relationship between NC and the development of CNS metastases is worth exploring, as the others have proposed15. In this study, none of the patients with NC developed simultaneous or asynchronous CNS metastasis. Perhaps, the excessive TH2 response seen in NC16 is responsible for that effect, in some extent. A series of certain HLA haplotypes, which have been considered to affect the susceptibility to NC infection17,18, will now be studied further at our institution. The estimated incidence of NC and cancer is not low and should be considered a differential diagnosis of brain metastases, especially in developing countries.